A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026599



Internal ID85470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104670509..104681531hg38UCSC Ensembl
chr9:107432790..107443812hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3811023
hg1911023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493668
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026599
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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